CRA I - Beijing
Clinical Careers Page(13 days ago)
About this role
The CRA I at Syneos Health supports clinical trial site management activities, ensuring regulatory compliance, data integrity, and subject safety. The role involves site qualification, monitoring, and collaboration with site personnel, with a focus on the clinical trial process from initiation to close-out, including real-world late phase studies.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Data Management
- Regulatory Compliance
- Source Document Review
- Investigational Product
- Protocol Adherence
- CRO
- Clinical Trials
Qualifications
- Bachelor’s Degree or RN in a related field
About Clinical Careers Page
syneoshealth.comSyneos Health is a biopharma solutions organization and full‑service contract research organization (CRO) that integrates clinical development, regulatory and commercialization services to help life‑science companies bring therapies to market faster. It provides end‑to‑end capabilities — clinical trials across phases and therapeutic areas, real‑world evidence and data analytics, medical affairs, market access, patient engagement and commercial launch services. With a global network of scientific, clinical and commercial experts, Syneos partners with biopharma, biotech and medtech clients to de‑risk development programs and accelerate product adoption.
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